Thermocyclops crassus Ecological Risk Screening Summary

Transcription

1 U.S. Fish and Wildlife Service Thermocyclops crassus Ecological Risk Screening Summary U.S. Fish and Wildlife Service, October 2016 Photo: Mesocyclops crassus [accepted as Thermocyclops crassus] from Sars, G.O. 1914, Plate 37. Licensed under CC BY-NC-SA. Available: (October 2016). 1 Native Range and Status in the United States Native Range From Reid (1989): present throughout the Palearctic, Australia, South and Southeast Asia, occurring most commonly in tropical Africa Status in the United States From Duchovnay et al. (1992): 1

2 The cyclopoid copepod Thermocyclops crassus was collected in Missisquoi Bay, Lake Champlain, Vermont, U.S.A., in May and August Since this is the first confirmed record of the species in North America, the population is considered to be introduced. The date of introduction of the Lake Champlain population is uncertain. Its localized distribution with the lake indicates that introduction was recent [ ] In spite of its inclusion in the widely used key of Yeatman (1959), T. crassus has not been reported in North America in recent decades. For this reason we do not believe that the species is presently distributed widely on this continent. Most published records of T. crassus from the Americas were found by Reid (1989) to refer to the similar pantropical species T. decipiens Kiefer Means of Introductions in the United States From Duchovnay et al. (1992): The origin and means of introduction are unknown. From Duggan et al. (2005): Here, we assess whether residual water and sediments of NOBOB [ no-ballast-on board ] ships provide an invasion risk to the Great Lakes. We examine the identity, abundances, and frequencies of live organisms associated with these residuals in NOBOB ships entering the Great Lakes. [ ] A total of 35 copepod species were identified from the 33 ships. [ ] Four species, Mesocyclops leuckarti, Paracyclops fimbriatus, Thermocyclops crassus, and Thermocyclops oithonoides, are freshwater species that do not have established populations in the Great Lakes. Remarks From Walter (2015): Synonymised names Mesocyclops brevifurcatus Harada, 1931 Mesocyclops crassus (Fischer, 1853) From Duchovnay et al. (1992): Because of the difficulty of discrimination of T. crassus and similar congeners, information on this species appears in the scientific literature under a confusing variety of names. Kiefer (1978) and Rylov [1948 (1963)] discussed its taxonomic history in detail and provided a list of synonyms, the most common of which is Thermocyclops (or Mesocyclops) hyalinus Rehberg Additional nomenclatural confusion has been caused by the former inclusion of species of Thermocyclops in the genus Mesocyclops, or, in older literature, Cyclops. From Reid (1989): 2

3 [As of 1989,] the only confirmed record of this species in the western hemisphere is that of Collado, Defaye et al. (1984[a]) from three small ponds in San Jose Province, Costa Rica [ ] B. H. Dussart, C. H. Fernando (in litt.) and co-workers (Collado, Fernando & Sephton, 1984[b]) agree that most published records of T. crassus in South and Central America and the Caribbean region refer to T. decipiens 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing From ITIS (2016): Kingdom Animalia Subkingdom Bilateria Infrakingdom Protostomia Superphylum Ecdysozoa Phylum Arthropoda Subphylum Crustacea Class Maxillopoda Subclass Copepoda Infraclass Neocopepoda Superorder Podoplea Order Cyclopoida Family Cyclopidae Genus Thermocyclops Kiefer, 1927 Species Thermocyclops crassus (Fischer, 1853) Current Standing: valid Size, Weight, and Age Range From NINA (2016): Female: Length mm Male: Length 0.7 mm From Duchovnay et al. (1992): Maturation time can be as short as a few weeks at tropical temperatures, with multiple generations per year (Lewis 1979), although in temperate waters, the species may have as few as two generations annually [Rylov 1948 (1963)]. Environment From Duchovnay et al. (1992): It has been collected from waters of ph , but the optimum ph is 7-8 [Rylov 1948 (1963)]. It is tolerant of salinities up to 7.2 o/oo (Löffler 1961). 3

4 Climate/Range From Tackx et al. (2004): T. crassus exhibits an optimal development around 25 C. At lower temperature, the rate of development decreases [ ] From Kobari and Ban (1998): In laboratory experiments, this species did not produce eggs below 10 C (Maier, [1989]). In the present study, reproduction of T.crassus also occurred at water temperatures >10 C in both ponds. This suggests that T.crassus is adapted to the warm season, and winter diapause of this species may be a strategy to avoid low temperature. Water temperature may be an important factor influencing the life cycle pattern of T.crassus Distribution Outside the United States Native From Reid (1989): present throughout the Palearctic, Australia, South and Southeast Asia, occurring most commonly in tropical Africa Introduced From Gutiérrez-Aguirre and Suárez-Morales (2000): A limnological survey carried out during January 1998 in the state of Tabasco, southeastern Mexico, established the occurrence of the Eurasian freshwater copepod Thermocyclops (Fischer, 1853) at several sites. It has been found in Costa Rica [ ] (Collado et al., 1984[a]; Reid, 1990; Reid & Pinto-Coelho, 1994), and has been recorded recently from Nicaragua (Reid, pers. comm.). Means of Introduction Outside the United States From Gutiérrez-Aguirre and Suárez-Morales (2000): The introduction of this eurytopic species in freshwater systems of Tabasco [Mexico] is probably related to aquacultural activities. Short description From NINA (2016): The body of T. crassus is rather short and stout and its furca is about twice as long as wide. The ratio between the outer and the inner setae attached to the furca [is] 1:3 [ ] Its colour is very pellucid with a faint yellowish tinge. 4

5 Biology From Duchovnay et al. (1992): [ ] occurring in large and small natural and artificial lakes and reservoirs, and occasionally in rivers [Kiefer 1978, Rylov 1948 (1963)]. The species is primarily pelagic but can also attain high populations among dense littoral immersed macrophytes [Flössner 1967, Rylov 1948 (1963)]. It is thermophilic and in more temperate regions comprises a significant component of the plankton only during the warmer months. In tropical climates this species is often among the dominant crustacean plankters (Fernando 1980, Hodgkiss 1977, Lewis 1979). [ ] It is herbaceous, feeding on diatoms, cryptomonads, and cyanophyceans (Fernando 1980, Lewis 1979), and thrives in mesotrophic and eutrophic waters [Patalas and Patalas 1966, Rylov 1948 (1963)]. [ ] Thermocyclops crassus may diapause as a CIV or CV copepodid. In several Italian lakes, T. crassus overwinters in the benthos as diapausing copepodid CV stages (Stella et al. 1972; E. Stella, personal communication to J. W. R., 1992), whereas in several German lakes, T. crassus overwinters as a CIV copepodid (Maier 1990). Human uses From Nam et al. (1998): In 1993, the World Health Assembly officially designated dengue control and prevention as a high priority [ ] However, success has been limited by a lack of effective methods to control the principal vector, Aedes aegypti (L.), an urban mosquito that breeds in water storage containers as well as discarded containers that collect rainwater. [ ] Herein we report the success of a relatively new control method: cyclopoid copepods. [ ] Predacious cyclopoids are particularly effective because of their broad diet, consisting of algae, protozoa, rotifers, and most aquatic animals up to their own size and because they do not depend on the supply of mosquito larvae. Diseases No information available. Threat to humans No information available. 3 Impacts of Introductions No information available. 5

6 4 Global Distribution Figure 1. Known global established locations of Thermocyclops crassus according to GBIF (2016). 5 Distribution within the United States Figure 2. Distribution of Thermocyclops crassus in the United States. Map from USGS (2016). 6

7 6 Climate Matching Summary of Climate Matching Analysis The climate match (Sanders et al. 2014; 16 climate variables; Euclidean Distance) was high in the Northeast, Great Lakes region, and much of California. Climate match was medium for the Mid-Atlantic region, much of the Midwest, and Florida. The Pacific Northwest and South-central U.S. exhibited low climate match. The Interior West was a patchwork of high, medium, and low climate matches. The Climate6 score for Thermocyclops crassus indicates a high climate match to the continental U.S. Climate6 scores of and greater indicate high climate match; Climate6 score for T. crassus was Figure 3. RAMP (Sanders et al. 2014) source map showing weather stations selected as source locations (red) and non-source locations (gray) for Thermocyclops crassus climate matching. Source locations from GBIF (2016) and Discover Life (2016). One source location in Russia from Discover Life (2016) was omitted because the locational accuracy could not be confirmed. Additional source locations in Nigeria from Jeje (1988), in Costa Rica from Reid (1989), in Japan from Kobari and Ban (1998), in Vietnam from Nam et al. (1998), in Mexico from Gutiérrez-Aguirre and Suárez-Morales (2000), in India from Kumar et al. (2011), and in the Philippines from Papa and Zafarella (2011). 7

8 Figure 4. Map of RAMP (Sanders et al. 2014) climate matches for Thermocyclops crassus in the continental United States based on source locations reported by Jeje (1988), Reid (1989), Kobari and Ban (1998), Nam et al. (1998), Gutiérrez-Aguirre and Suárez-Morales (2000), Kumar et al. (2011), Papa and Zafarella (2011), Discover Life (2016), and GBIF (2016). 0= Lowest match, 10=Highest match. 7 Certainty of Assessment Limited information is available on the distribution and biology of Thermocyclops crassus and no information is available on impacts of introductions. More research will be necessary to determine the impact of this species where it has been introduced in North and Central America. Certainty of this assessment is low. 8 Risk Assessment Summary of Risk to the Contiguous United States Thermocyclops crassus is a cyclopoid copepod native to Eurasia, Africa, and Australia. In the Americas, it has a highly localized distribution in Costa Rica, Nicaragua, Mexico, and the U.S. (Lake Champlain), assumed to be the result of recent introductions. Difficulty in identifying this 8

9 species has resulted in other erroneous reports of T. crassus in the Americas. Current research on T. crassus is focused on describing its distribution and basic biology, and no impacts of introductions have yet been reported. T. crassus has been observed in residual ballast water in ships arriving in the Great Lakes, raising the possibility of transoceanic shipping as an introduction pathway, although the means of past introductions are unknown. T. crassus has a high climate match to the continental United States, particularly in the Northeast, Great Lakes region, and California. While these locations of high climate match are quite different in terms of temperature and precipitation, the climate match may be responding to a combination of any of 16 different climate variables included in the matching process. Additionally, climate match to the continental U.S. may be underestimated, given that T. crassus is broadly distributed across Europe, Africa, Asia, and Australia, and likely not limited to the locations pinpointed in climate matching. Overall risk posed by this species is uncertain. Assessment Elements History of Invasiveness (Sec. 3): None Documented Climate Match (Sec.6): High Certainty of Assessment (Sec. 7): Low Overall Risk Assessment Category: Uncertain 9 References Note: The following references were accessed for this ERSS. References cited within quoted text but not accessed are included below in Section 10. Discover Life Thermocyclops crassus. Discover Life. Available: (October 2016). Duchovnay, A., J. W. Reid, and A. McIntosh Thermocyclops crassus (Crustacea: Copepoda) present in North America: a new record from Lake Champlain. Journal of Great Lakes Research 18(3): Duggan, I. C., C. D. A. van Overdijk, S. A. Bailey, P. T. Jenkins, H. Limén, and H. J. MacIsaac Invertebrates associated with residual ballast water and sediments of cargocarrying ships entering the Great Lakes. Canadian Journal of Fisheries and Aquatic Sciences 62: GBIF (Global Biodiversity Information Facility) GBIF backbone taxonomy: Thermocyclops crassus (Fischer, 1853). Global Biodiversity Information Facility, Copenhagen. Available: (October 2016). Gutiérrez-Aguirre, M., and E. Suárez-Morales The Eurasian Thermocyclops crassus (Fischer, 1853) (Copepoda, Cyclopoida) found in southeastern Mexico. Crustaceana 73(6):

10 ITIS (Integrated Taxonomic Information System) Thermocyclops crassus (Fischer, 1853). Integrated Taxonomic Information System, Reston, Virginia. Available: (October 2016). Jeje, C. Y A revision of the Nigerian species of the genera Mesocyclops Sars, 1914 and Thermocyclops Kiefer, 1927 (Copepoda: Cyclopoida). Hydrobiologia 164: Kobari, T., and S. Ban Life cycles of two limnetic cyclopoid copepods, Cyclops vicinus and Thermocyclops crassus, in two different habitats. Journal of Plankton Research 20: Kumar, P., A. Wanganeo, R. Wanganeo, F. Sonaullah Seasonal variations in zooplankton diversity of Railway pond, Sasaram, Bihar. International Journal of Environmental Sciences 2(2): Nam, V. S., N. T. Yen, B. H. Kay, G. G. Marten, and J. W. Reid Eradication of Aedes aegypti from a village in Vietnam, using copepods and community participation. American Journal of Tropical Medicine and Hygiene 59(4): NINA (Norwegian Institute for Nature Research) Thermocyclops crassus (Fischer 1853). Norwegian Institute for Nature Research, Trondheim, Norway. Available: Infomateriell/2007/krepsdyrfaktaark/walseng_Thermocyclops%20crassus.pdf. (October 2016). Papa, R. D. S., and M. T. Zafaralla The composition, diversity and community dynamics of limnetic zooplankton in a tropical caldera lake (Lake Taal, Philippines). The Raffles Bulletin of Zoology 59(1):1-7. Reid, J. W The distribution of species of the genus Thermocyclops (Copepoda, Cyclopoida) in the western hemisphere, with description of T. parvus, new species. Hydrobiologia 175: Sanders, S., C. Castiglione, and M. H. Hoff Risk Assessment Mapping Program: RAMP. U.S. Fish and Wildlife Service. Tackx, M. L. M., N. de Pauw, R. van Mieghem, F. Azémar, A. Hannouti, S. van Damme, F. Fiers, N. Daro, and P. Meire Zooplankton in the Schelde estuary, Belgium and The Netherlands. Spatial and temporal patterns. Journal of Plankton Research 26(2): USGS (U.S. Geological Survey) Thermocyclops crassus. USGS Nonindigenous Aquatic Species Database, Gainesville, Florida. Available: (October 2016). 10

11 Walter, T. C Thermocyclops crassus (Fischer, 1853). In T. C. Walter, and G. Boxshall. World of copepods database. Available: (October 2016). 10 References Quoted But Not Accessed Note: The following references are cited within quoted text within this ERSS, but were not accessed for its preparation. They are included here to provide the reader with more information. Collado, C., D. Defaye, B. H. Dussart, and C. H. Fernando. 1984a. The freshwater Copepoda (Crustacea) of Costa Rica with notes on some species. Hydrobiologia 119: Collado, C., C. H. Fernando, and D. Sephton. 1984b. The freshwater zooplankton of Central America and the Caribbean. Hydrobiologia 113:105-l 19. Fernando, C. H The species and size composition of tropical freshwater zooplankton with species reference to the Oriental Region (South East Asia). Internationale Revue der Gesamten Hydrobiologie 65: Flössner, D Beitrag zur Kenntnis der Cladocerenund Copopodenfauna des Donaudeltas. Limnologica 5: Hodgkiss, I. J The use of simultaneous sampling bottle and vertical net collections to describe the dynamics of a zooplankton population. Hydrobiologia 52: Kiefer, F Freilebende Copepoda. Binnengewässer 26(2), Zooplankton der Binnengewässer 2: Lewis, W. M. Jr Zooplankton community analysis: studies on a tropical system. Springer- Verlag, New York. Löffler, H Beiträge zur Kenntnis der Iranischen Binnengewässer II. Regionallimnologische Studie mit besonderer Berücksichtingung der Crustaceenfauna. Internationale Revue der Gesamten Hydrobiologie 46: Maier, G The effect of temperature on the development times of eggs, naupliar and copepodite stages of five species of cyclopoid copepods. Hydrobiologia 184: Maier, G Spatial distribution of resting stages, rate of emergence from diapause and times to adulthood and to the appearance of the first clutch in 3 species of cyclopoid copepods. Hydrobiologia 206:

12 Patalas, J., and K. Patalas The crustacean plankton communities in Polish lakes. Verhandlungen des Internationalen Verein Limnologie 16: Reid, J. W Continental and coastal free-living Copepoda (Crustacea) of Mexico, Central America and the Caribbean region. Pages in D. Navarro, and J. Robinson, editor. Diversidad biológica en el reserva de la Biósfera de Sian Ka'an Quintana Roo, México. Centro de Investigaciones de Quintana Roo, Mexico. Reid, J. W., and M. Pinto-Coelho An Afro-Asian continental copepod, Mesocyclops ogunnus, found in Brazil; with a new key to the species of Mesocyclops in South America and a review of intercontinental introductions of copepods. Limnologica 24(4): Rylov, V. M (1963). Freshwater Cyclopoida. Fauna USSR, Crustacea 3(3): National Science Foundation, Washington, D.C. and Israel Program for Scientific Translation, Jerusalem. (English translation.) Stella, E., F. G. Margaritora, G. B. Palmegiano, and M. Bazzanti Il Lago di Martignano: prime osservazioni sulla struttera e distribuzione delle biocenosi. Accademia Nazionale dei XL, Section 4 22:3-17. Yeatman, H. C Free-living Copepoda: Cyclopoida. Pages in W. T. Edmondson, editor. Ward & Whipple s fresh-water biology, 2nd edition. Wiley, New York. 12